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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2007 3
2008 3
2009 2
2010 4
2012 2
2013 2
2014 2
2015 3
2016 3
2017 4
2018 3
2019 1
2020 5
2021 3
2022 3
2023 2
2024 0

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39 results

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Page 1
Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of KATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC. Ngoc CTB, et al. Among authors: dung vc. Front Endocrinol (Lausanne). 2021 Sep 9;12:727083. doi: 10.3389/fendo.2021.727083. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34566892 Free PMC article.
The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.
Germain DP, Moiseev S, Suárez-Obando F, Al Ismaili F, Al Khawaja H, Altarescu G, Barreto FC, Haddoum F, Hadipour F, Maksimova I, Kramis M, Nampoothiri S, Nguyen KN, Niu DM, Politei J, Ro LS, Vu Chi D, Chen N, Kutsev S. Germain DP, et al. Among authors: vu chi d. Mol Genet Genomic Med. 2021 May;9(5):e1666. doi: 10.1002/mgg3.1666. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33835733 Free PMC article. Review.
We All Have a Role to Play: Redressing Inequities for Children Living with CAH and Other Chronic Health Conditions of Childhood in Resource-Poor Settings.
Armstrong K, Benedict Yap A, Chan-Cua S, Craig ME, Cole C, Chi Dung V, Hansen J, Ibrahim M, Nadeem H, Pulungan A, Raza J, Utari A, Ward P. Armstrong K, et al. Among authors: chi dung v. Int J Neonatal Screen. 2020 Sep 25;6(4):76. doi: 10.3390/ijns6040076. Int J Neonatal Screen. 2020. PMID: 33124614 Free PMC article.
39 results